Sanmeng corrected reference serum
- Analysis ID
- 584b49d0685f29d05ccab2ede0a11158
- Customs Code
- DHA00601633004
- Manufacturer
- THERMO ELECTRON CORPORATION
- Manufacturer Country
- Australia
- Authorized Representative
- MEDICARE PRODUCTS INC.
- Intended Use
- It is used for the second correction on the clinical chemical analysis instrument.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1150 Calibrated Products
- Import Information
- import
- Registration Date
- Apr 11, 2006
- Expiry Date
- Apr 11, 2011
- Cancellation Date
- Oct 29, 2012
- Status
- Logged out
- Reason
- 許可證已逾有效期
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Access comprehensive regulatory information for Sanmeng corrected reference serum in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 584b49d0685f29d05ccab2ede0a11158 and manufactured by THERMO ELECTRON CORPORATION. The authorized representative in Taiwan is MEDICARE PRODUCTS INC..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including FISHER DIAGNOSTICS, A DIVISION OF FISHER SCIENTIFIC COMPANY, LLC, A SUBSIDIARY OF THERMO FISHER, and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.